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13 часов назад

Associate Director, Central Monitor (Clinical Research)

141 500 - 268 500$
Формат работы
hybrid
Тип работы
fulltime
Грейд
director
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Associate Director, Central Monitor (Clinical Research): Leading Central Monitoring Managers and de-risking assigned clinical studies across AbbVie clinical research and development programs with an accent on risk-based monitoring, staffing strategy, service delivery, and leadership development. Focus on managing a portfolio of studies, building the central monitoring leadership pipeline, and driving analytical decision-making across cross-functional teams.

Location: Hybrid role with on-site work Tuesday through Thursday; candidates must be local to Lake County, IL, Irvine, CA, or Florham Park, NJ.

Salary: $141,500–$268,500 annually.

Company

hirify.global develops innovative medicines and healthcare solutions across areas including immunology, oncology, neuroscience, and aesthetics.

What you will do

  • Lead, manage, and supervise Central Monitoring Managers responsible for delivering a portfolio of clinical studies.
  • Develop and execute central monitoring staffing strategies aligned with study priorities, timelines, quality, and efficiency objectives.
  • Build the leadership talent pipeline through recruitment, hiring, training, coaching, and mentoring.
  • Manage performance cycles, set objectives, provide timely feedback, and resolve performance issues.
  • Collaborate with Clinical Development Operations and cross-functional stakeholders to achieve high standards of delivery.
  • Promote risk-based quality management and the early detection of issues to de-risk clinical studies.

Requirements

  • Bachelor's degree in a related field, such as life sciences or a risk-based discipline.
  • At least 10 years of clinically related experience or data trend analysis experience, including at least 5 years of people management.
  • Required experience with an RBQM model or similar risk-based monitoring experience.
  • Experience with drug development, clinical operations, risk management, strategic execution, and decision-making.
  • Experience managing remote or virtual teams and influencing stakeholders in a cross-functional global environment.
  • Strong spoken, written, and conversational English is required, along with the ability to work on-site three days per week in one of the specified US locations.

Culture & Benefits

  • Inclusive, collaborative, innovative, and continuous-improvement-oriented work environment.
  • Paid vacation, holidays, and sick leave.
  • Medical, dental, and vision insurance for eligible employees.
  • 401(k) plan for eligible employees.
  • Eligibility to participate in short-term incentive programs.

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